Employment Type : Full-Time
Clinical Research Coordinator 1 Position Description Alliance for Multispecialty Research is a fast-growing clinical research organization that conduct trials for the development of pharmaceuticals. AMR offers competitive pay, 401K matching, health/dental/vision, paid STD and LTD, as well as on demand access to your pay! Team Member Benefits: · Health, Dental, Vision · Supplemental Life Coverage · Short-term Disability and Long-term Disability (AMR covers cost) · Life Insurance (AMR covers cost of AD&D $50,000) · 401K (employer matching) · Paid Time Off · Holiday Pay · Employee Assistance Program Position Overview The Clinical Research Coordinator I will perform multiple and varied tasks critical to the management of clinical research studies. The Clinical Research Coordinator I is expected to exhibit basic knowledge of clinical research activities and adhere to federal and other applicable regulations. The Clinical Research Coordinator I must ensure compliance with protocol guidelines, identify problems and/or inconsistencies and monitor subject process throughout the clinical research study. To consistently embody AMR’s Core Values: · Excellence and Consistency · Collaborative Innovation · Respect for our Subjects, Sponsors and Team Members · Community · Unimpeachable Ethics The Clinical Research Coordinator reports to the Clinical Operations Manager. Classification: Non-Exempt Primary Responsibilities: · Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols. · Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study. · Basic understanding of medications per clinical trial. · Acquire detailed knowledge of the protocol and procedures associated with each clinical research study. · Effectively communicate with clinical research sponsors, CROs, monitors/CRAs, IRBS, laboratories and clinical personnel within the research industry. · Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research study. · Notify Investigator, monitor/CRA of any adverse events or serious adverse events per the protocol. · Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately. · Complete all required documentation in a legible and timely fashion. · Ensure all necessary documents are appropriately signed and dated. · Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed. Desired Skills and Qualifications: · Successful completion of a formal medical/clinical educational program or in the alternative has a strong knowledge of medical terminology and the ability to learn quickly. · Clinical experience involving patient care in a healthcare environment preferred but not required. · Ability to interpret and perform clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred. · Ability to function independently with minimal supervision, and to exercise discretion and a high level of good clinical and other professional judgement. · Ability to multi-task and perform multiple critical tasks simultaneously (under dynamic and ever-changing conditions and deadlines). · Exceptional written and verbal communication skills. · Ability to work independently, lead clinical research studies and complete tasks. · Calm, friendly, approachable, and presents a professional image. · Excellent listening, written, and verbal communication skills. · Committed, highly energetic, self- motivated and highly organized. · Demonstrated proficiency in office equipment including (but not limited to) copy machines, facsimile machine, multi-line telephones and computers. · Proficient in Microsoft Office products including Outlook, Word, and Excel. · Professional and highly motivated “self-starter” with the ability to exercise initiative. · Excellent task management and prioritization skills. Job Type: Full-time Pay: $40,000.00 - $55,000.00 per year Benefits: Schedule: Education: Experience: Work Location: One location